Canonical Allele Identifier: CA1085301553
Gene:

Linked Data

dbSNP Id: rs1761318842
gnomAD v3: 6-1535833-GC-G
gnomAD v4: 6-1535833-GC-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1535835del , CM000668.2:g.1535835del GRCh38
NC_000006.11:g.1536070del , CM000668.1:g.1536070del GRCh37
NC_000006.10:g.1481069del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_427861.2:n.234+16512del
XR_926380.1:n.218-2621del
XR_926381.1:n.1108-2621del
XR_926382.1:n.235-6655del
XR_926384.1:n.200-6655del
XR_001743921.1:n.235-6679del
XR_427861.3:n.234+16512del
XR_926381.2:n.1123-2621del